Certain 4-amino-6-aryl-pyrimidines

ABSTRACT

4-AMINO-6-ARYLPYRIMIDIENES AND SALTS THEREOF, A NOVEL CLASS OF INHIBITORS OF PLATELET AGGREGATION AND BRONOCHODILATORS IN MAMMALS.

United States Patent 3,707,560 CERTAIN 4-AMINO-6-ARYL-PYRIMIDIWES Gerald George De Angelis, Wilton, and Hans-Jurgen Ernst Hess, Old Lyme, Conn., assignors to Pfizer Inc., New York, N.Y. No Drawing. Filed Oct. 5, 1970, Ser. No. 78,216 Int. Cl. C0711 51/42 US. Cl. 260256.5 R 19 Claims ABSTRACT OF THE DISCLOSURE 4-amino-6-arylpyrimidines and salts thereof, a novel class of inhibitors of platelet aggregation and bronchodilators in mammals.

BACKGROUND OF THE INVENTION This invention relates to 6-arylpyrimidines, and more particularly to a series of 4-substituted amino derivatives and salts thereof and to the use of said agents as inhibitors of platelet aggregation and bronchodilators in mammals.

The synthesis of 4-amino-o-phenylpyrimidine has been reported by Bredereck, etc., Chem. Ber. 90, 942 (1957), and by van der Plas, et al., Tetrahedron Lett., No. 31, 2093 (1964), with no disclosure of utility. The preparation, also without mention of use, of 4-amin0-6-(p-tbutylphenyl)pyrimidine was reported by van der Plas, Rec. Trav. Chim., 84, 1101 (1965).

Khrornov-Borinov, Sokl. Ahad. Nauk USSR, 180, 1129 (1968) has reported properties of 4-amino-6-methylpyrimidine with no utility disclosure.

SUMMARY OF THE INVENTION 1 Are W2 and the acid addition salts thereof, wherein:

Ar is selected from the group consisting of phenyl; monosubstituted phenyl wherein said substituent is methyl, methoxy, 3,4-dimethoxy, hydroxy, trifluoromethyl, fluorine, chlorine, bromine, carboxy, cyano, nitro, dialkylamino said alkyl containing from 1 to 3 carbon atoms, amino or acylamino containing from 1 to 4 carbon atoms; pyridyl; thienyl; furyl; monosubstituted pyridyl, thienyl or furyl wherein said substituent is acylamino containing from 1 to 4 carbon atoms; naphthyl; 3-indolyl; 2- and 3-benzothienyl; and 2- and 3-benzofuryl;

R and R are each selected from the group consisting of hydrogen; alkyl containing from 1 to 4 carbon atoms; substituted ethyl wherein said substituent is selected from the group consisting of Z-dimethylamino, 2-hydroxy and 2,2,2-trifluoro; alkenyl containing from 3 to 4 carbon atoms; pyridylmethyl; 2-monosubstituted ice phenyl wherein said substituent is carboxy or sulfamoyl; and cycloalkyl containing from 3 to 7 carbon atoms;

R and R when taken together with the nitrogen atom to which they are attached form a heterocyclic ring of the formula:

wherein Z is selected from the group consisting of CH 0, S and N-alkyl containing from 1 to 3 carbon atoms; and n and m are integers of from 2 to 3.

Of particular interest, because of their potency for inhibition of platelet aggregation, are compounds wherein R and R are each hydrogen, alkyl up to 4 carbon atoms and substituted ethyl where said substituent is Z-hydroxy or 2,2,2-trifluoro and Ar is phenyl or monosu'bstituted phenyl.

In addition to their activity as inhibitors of platelet aggregation several compounds of the instant invention are potent relaxants of smooth muscle and in particular bronchial tissue. Of particular interest as bronchodilators are congeners where R and R are alkyl of up to 4 carbon atoms and Ar is acylamino-substituted phenyl.

DETAILED DESCRIPTION OF THE INVENTION In accordance with the process employed for the preparation of compounds of the instant invention, several alternate synthetic methods are used. The first synthetic route, Method A, is illustrated by the following scheme:

(III) N Ar 7 III RlRzNH In the first reaction step of the aforementioned scheme, an aryl Grignard is contacted with an ester of cyanoacetate in a reaction inert solvent. In practice, the aryl Grignard, generated in situ from the aryl halide and magnesium turnings in a solvent such as ether, is treated with an ester of cyanoacetate, generally the methyl or ethyl ester, in the same solvent. It'is desirable to use at least a 200% excess of the requisite Grignard reagent to effect a maximum yield of product.

The aforedescribed reaction is carried out at ambient temperatures for several hours followed 'by subsequent hydrolysis of the reaction mixture with dilute sulfuric acid and extraction of the amino ester into the ether phase. Removal of the solvent is followed by purification by distillation if the product (I) is an oil or recrystallization when a solid.

Alternately, an aryl lithium salt can be used in place of the Grignard reagent without markedly affecting the course of the reaction.

The requisite Grignard reagents are available commercially or can be synthesized from the corresponding aryl halide, which are commercial products, by methods available to those skilled in the art, e.g., as outlined by Kharasch, et al., Grignard Reactions of Nonmetallic Substances, Prentice-Hall, New York, 1954.

Cyclization of the fl-amino arylacrylic esters (I) to the 4-hydroxy-6-arylpyrimidines (H) is carried out in a highly polar, reaction-inert solvent such as dimethylsulfoxide or dimethylformamide employing a five to ten fold excess of formamide and at least two equivalents of an alkali metal lower alkoxide such as potassium t-butoxide or sodium ethoxide. Temperatures of from 75l0() C. are employed with reaction times of -24 hours. Isolation of the desired product is carried out by pouring the reaction mixture onto ice followed by acidification with glacial acetic acid. Further purification is effected by recrystallization from a suitable solvent.

The action of halogenating agents such as thionyl chloride, phosphorous oxychloride or phosphorous pentachloride converts the 4-hyrdoxy-6-arylpyrimidines (H) to the 4-chloro analog (IH). Experimentally, II is added to a large excess of the chlorinating reagent, preferably phosphorous oxychloride, and the mixture heated to reflux from 1 to 2 hours. Lower temperatures can be employed with correspondingly longer reaction times. After removed of excess reagent in vacuo, the residual product is poured into a mixture of ammonium hydroxide and ice. The crude product can be used in the next reaction or may be further purified via recrystallization.

Displacement of the 4-chloro substituent of compounds of Formula 111, leading to the products of the present invention, is carried out in a reaction-inert solvent, e.g., ethanol or tetrahydrofuran with ammonia or an amine, HNR R wherein R and R are as previously described. Alternately, the reaction can be carried out neat, i.e., without solvent. In practice, at least 2 moles of ammonia or amino per mole of III is employed, and as much as a fold excess can be employed. It is generally advantageous to heat the aforementioned reaction from about 50-100 C. per periods of 2-8 hours. Work-up of the reaction constitutes pouring the mixture into water followed by extraction of IV into a non-aqueous solvent such as chloroform and subsequent conversion of the free base to a suitable salt, e.g., hydrochloride, by treating a solution of said base with the appropriate acid.

Also within the scope of this invention are compounds of Formula IV wherein a methyl or ethyl substituent exists at the 2- and/or S-positions. Provisions for introducing a substituent at the 5-position are made in the first step of this sequence of reactions wherein an a-methyl or a-ethyl cyano-acetate ester is reacted with the appropriate aryl Grignard or organolithium compounds. Introduction of the methyl or ethyl substituent into the Z-position requires the use of acetamide or propionamide in place of formamide in the second step of the described sequence. In general, the substitution of the aforementioned starting materials does not markedly affect the course or yields of the reactions involved.

Method A is particularly applicable to the preparation of compounds of Formula IV wherein R and R are as previously described and where Ar is pyridyl, thienyl, furyl, naphthyl, 3-indolyl, 2- and 3-benzothienyl, 2- and 3-benzofuryl, phenyl and monosubstituted phenyl where said substitutents are methyl, methoxy, 3,4-dimethoxy, trifluoromethyl, fluorine, chlorine and bromine.

Also within the purview of this invention are congeners of IV wherein Ar includes 3,4-methylenedioxyphenyl, acetylphenyl and disubstituted phenyl where the second substituent is selected from the group consisting of methyl, methoxy, fluorine, chlorine and bromine.

The first alternate series of reactions, Method B, leading to the products of the present invention, is outlined as follows NHn \ s 0 02 CH;

CN Nasal-120020113 In the first reaction of the aforementioned Method B an appropriately substituted o-chlorobenzonitrile is contacted with a salt of a lower alkyl thioglycolate ester in a reaction-inert solvent. In practice, sodium methyl thioglycolate, prepared by treating methyl thioglycolate with an equivalent amount of sodium alkoxide in a lower alkanol solvent followed by removal of the solvent in vacuo, is added to a reaction-inert solvent, preferably of moderately high polarity, e.g., dimethylformamide or hexamethylphosphoramide. The resulting solution or suspen- S1011 of sodium methyl thioglycolate is treated with an equimolar amount of the requisite o-chlorobenzonitrile dissolved in the same solvent.

Alternately, the sodium salt of the methyl thioglycolic can be generated in situ in said reaction employing either an equimolar amount of sodium hydride or a sodium alkoxide.

The aforedescribed reaction is carried out at 50l00 C. for a period of 15 minutes to 2 hours. A convenient method of isolation is to cool the reaction mixture and subsequently add it to a mixture of ice and water. The desired product can be filtered, dried, and recrystallized from a suitable solvent.

The requisite o-chlorobenzonitriles are available commercially or can be synthesized by one skilled in the art, e.g., by the method of Nakaoka, et al., German Pat. No. 1,230,026 (CA. 66 55255e).

Cyclization of the 2-carbomethoxy-3-aminobenzothiophenes (V) to the tricyclic 4-hydroxybenzothieno[3,2- d]pyrimidines (VI) is carried out in a reaction-inert solvent such as dimethylsulfoxide or dimethylformamide using a 5 to fold excess of formamide and an equimolar amount of an alkali metal lower alkoxide such as sodium methoxide or potassium t-butoxide. Reaction temperatures of 75-100 C. are employed with a reaction time of minutes to 2 hours. The desired product is isolated by pouring the cooled reaction mixture into water followed by acidification with acetic acid, filtration and drying. The product can be further purified by trituration or recrystallization from a suitable solvent.

The action of halogenating agents, e.g., thionyl chloride, phosphorous oxychloride or dichlorophenylphosphine oxide converts the 4-hydroxybenzothieno[3,2-d]pyrimidines (VI) to the corresponding 4-chloro analogs (VII). In practice, V1 is added to a large excess of the appropriate reagent, preferably phosphorous oxychloride, and the mixture heated. Reflux temperatures are preferred, although lower temperatures may be employed with correspondingly longer reaction times. The reaction period is not critical, but Will vary with temperature, concentration and reactivity of the starting reagents. In general, a period of from about 2 to about 8 hours is operable. A convenient method of isolation comprises removal of the excess phosphorous oxychloride in vacuo followed by treatment of the residue with water and sufficient ammonium hydroxide solution to render the solution basic. The resulting product is filtered and air dried. It can be used in this crude state for subsequent reaction or can be recrystallized from an appropriate solvent.

Displacement of the 4-chloro substituent of compounds of Formula VII, leading to VIII, is effected in a reactioninert solvent with ammonia or an amine, HNRyR wherein R and R are as previously described. In practice, a mixture of the appropriately substituted 4-chlorobenzothieno[3,2-d]pyrimidine and ammonia or a suitable amine are heated in a solvent such as ethanol, dimethylformamide, benzene or tetrahydrofuran. It is advantageous to employ at least 2 moles of amine per mole of halide, and as much as a 10 fold excess can be employed. It is generally desirable to heat the aforementioned reaction mixture to temperatures from about -l50 C., with a preferred range of 75-100 C. Reaction times are not critical, and will vary with reaction temperature, molar quantities of reactants, etc. In general, periods of 1 to 6 hours are operable.

Isolation of the products following the aforedescribed reaction is most conveniently carried out by diluting with water followed by extraction with a water immiscible solvent, e.g., chloroform, ether or benzene. The separated, non-aqueous phase is then dried over a suitable drying agent and the solvent removed in vacuo.

The final reaction of Method B, leading to the products of the present invention, comprises desulfurization of the 4-aminobenzothieno[3,2-d1pyrimidines (VIII) using an excess of Raney nickel. Experimentally, the reaction is carried out in a highly polar, reaction-inert solvent such as dimethylformamide and at temperatures of -150 C. Reaction times are not critical, but the preferred range is from 24-48 hours. Removal of the spent Raney nickel followed by concentration of the filtrate to dryness provides the crude free base of the desired product, which is converted to hydrochloride salt by conventional methods. Products isolated by Method B prove to be identical with those synthesized by Method A.

The aforedescribed method is particularly useful for the preparation of products of the instant invention wherein R and R are as previously described and Ar is phenyl and monoor disu'bstituted phenyl where said substituent is methyl, methoxy, 3,4-dimethoxy, cyano or carboxy.

The third alternate approach to the synthesis of compounds of the present invention (Method C) is outlined in the following scheme:

o o N a 5 (NH2)2CS At] SE Aron. -oo2rr5 0 N X Raney Nickel d A N P001 Id N N m HNR1R2 d /N\ R, R,

The initial step in the reaction sequence of Method C is a condensation of a (lower)alkyl aroylacetate with thiourea resulting in the formation of a 4-hydroxy-2-mcrcapto-G-arylpyrimidine (IX). In practice, the requisite ,8- ketoester is contacted with approximately equimolar amounts of thiourea in a reaction-inert solvent such as those represented by the (lower)alkanols. Temperatures of 60-90 C. are operable with corresponding reaction times of about 96-140 hours. Isolation of the desired product is achieved by concentration of the reaction mixture in vacuo followed by dilution with water, acidification to pH 3, cooling and, finally, filtration in the crude solids.

Alternately, S-methylisothiourea may also be employed in place of urea in the above described reaction and provides the corresponding Z-methylthio analog of IX.

The aroylacetates are either commercial products or can be conveniently synthesized by methods available to those skilled in the art, e.g., according to those extensively outlined by Hauser, et al., in Organic Reactions, John Wiley & Sons, Inc., New York, 1954, Chapter 9, p. 266.

Desulfurization of IX in aqueous sodium hydroxide using Raney nickel results in the formation of the corresponding 4-hydroxy-6-arylpyrimidine (II), identical to that prepared by Method A. Similarly, when the corresponding S-methyl analog of 1V is employed, identical products are obtained.

The subsequent steps of the reaction sequence, Method C, and corresponding results are identical to those of Method A.

Method C is especially useful for the preparation of compounds of the instant invention where R and R are as indicated previously and where Ar is phenyl or monoor disubstituted phenyl said substituents being cyano, methyl, methoxy, carboxy, acylamino or dialkylamino, pyridyl, furyl and acylamino substituted pyridyl and furyl, 3-indolyl, naphthyl and 2- and 3-benzofuryl.

Further, the use of an u-methylor m-ethylaroylacetate in the initial reaction of Method C, allows the synthesis of S-methyl or ethyl congeners of the final products (IV). Substitution of acetamide or propionamidine for thiourea leads to analogs of IV bearing a Z-methyl or 2-ethyl substituent.

Introduction of a nitro substituent into the aryl moiety of the 4-amino-6-arylpyrimidines can be carried out by direct nitration employing a mixture of nitric and sulfuric acids. In practice, to a solution of the substrate in concentrated sulfuric acid is added, dropwise and at room temperature, nitric acid. The resulting reaction is carried out at ambient temperature for about 2-6 hours. The reaction is quenched with ice, made basic with ammonium hydroxide and the free base extracted into a water immiscible solvent such as chloroform or methylene chloride.

In general, more than one nitroisomer is formed as a result of direct nitration. These isomers can subsequently be separated by conventional methods known to those skilled in the art, e.g., by fractional crystallization or column chromatography. Identification of said isomers is most conveniently carried out using nuclear magnetic resonance studies.

Treatment of the aforedescribed nitro compounds with reducing agents, such as stannous chloride and hydrochloric acid, results in the preparation of the corresponding amino analogs. Stannous chloride reductions are carried out at temperatures of -75 C. with reaction times of 2 to 4 hours, and preferably employ 12 N hydrochloric acid. The product, which is frequently sparingly soluble as the dihydrochloride salt in 12 N hydrochloric acid, is filtered from the cooled reaction mixture and the free base liberated by treatment of the salt with an aqueous base such as sodium hydroxide solution.

In addition to the aforementioned method of reducing nitro substituetns, several other reducing reagents, known to those skilled in the art, can be employed with comparable results, e.g., tin-hydrochloric acid, hydrogen-plat ium oxide, or aluminum amalgam.

4-amino 6 aminoarylpyrimidines, resulting from the above-mentioned reduction of the corresponding nitro compounds, can subsequently be reacted with a wide variety of reagents, including alkanoyl halides, anhydrides, alkyl halides, sulfonyl halides, isocyanates and thioisocyanates.

Reaction of said amino compounds with alkanoyl halides and alkoxycarbonyl halides leads to the preparation of the corresponding acylamino and alkyl carbamates, respectively. In practice, the alkanoyl or alkoxycarbonyl halide is added dropwise to a mixture of the appropriate amino compound and an alkali metal carbonate in a suitable reaction-inert solvent such as benzene, ether or methylene chloride. The reaction is preferably carried out at ambient temperatures for a reaction period of about 12 to 24 hours. Hydrolysis of the reaction with water and separation of the water immiscible solvent leads to the subsequent isolation of the crude product.

Analogously, sulfonyl halides are reacted under simi- 8 lar conditions and give rise to the corresponding sulfonamides.

Formation of acylamino substituents employing simple anhydrides or mixed anhydrides in place of aroyl or alkanoyl halides can be carried out with equal ease. Experimentally, the amino compound is contacted with at least an equimolar amount of the requisite anhydride and preferably a 20-50% excess. A solvent, such as benzene, pyridine, chloroform or tetrahydrofuran, can be employed, or the reaction can be run neat, i.e., Without solvent. In the latter case it is desirable to use as much as a IOU-300% excess of the appropriate anhydride. Said reaction is carried out for 12 to 24 hours at ambient temperatures. The excess anhydride can be removed under reduced pressure and the residue dissolved in ethyl acetate after which it is converted to the desired salt or alternately, the original reaction mixture can be diluted with ethyl acetate and the salt prepared directly by conventional methods.

Reaction of 4-amino-6-aminoarylpyrimidines with isocyanates and isothiocyanates gives rise to the corresponding ureas and thioureas. Said reactions are effected with the appropriate amino substrate and an equimolar amount, plus as much as a 20% excess, of the requisite isocyanate or thioisocyanate in a reaction-inert solvent, e.g., ether, tetrahydrofuran or benzene. Reaction times of about 12 to 24 hours at room temperature are generally adequate. Isolation of the desired product is achieved by removal of the solvent under reduced pressure followed by recrystallization of the residue from a suitable solvent.

Synthesis of 6-(N-alkylaminoaryl)pyrimidines and 6- (N,N-dialkylaminoaryl)pyrimidines is conveniently carried out by direct alkylation of the 6-aminoarylpyrimidines using an appropriate alkyl halide. The extent of alkylation is controlled by the relative amount of alkyl halide, generally the iodide, to the amino compound employed. For mono alkylation equimolar quantities of the two reactants are used plus a small, 10%, excess of the alkyl halide; dialkylation requires at least two moles of halide per mole of amino substrate. Allylic halides and aralkyl halides can also be used with similar ease.

In practice, a solution or suspension of the aminoarylpyrimidine and at least an equimolar amount of an alkali metal carbonate is treated with the appropriate alkyl halide, preferably the iodide, in the amounts previously described. The solvents for this alkylation can vary in nature and are selected from the group including (lower) alkanols, N,N-di(lower)alkyl (lower)alkylcarboxarnides, cyclic ethers and water. Elevated temperatures of from 50-110" C. are employed, with reaction times of 1-8 hours. The product is isolated by evaporation of the reaction solvent in vacuo followed by extraction of the residue with such solvents as methylene chloride or chloroform or, alternately, when water is used as the reaction solvent the product can be extracted from the mixture directly using said solvents. The separated extracting solvent is evaporated to dryness and the crude product purified by recrystallization from a suitable solvent or chromatographing on a silica gel column.

Also considered within the scope of the present invention are congeners wherein R and R when considered together with the nitrogen atom to which they are attached form a piperazine ring of the formula where X is (lower)alkyl, (lower)alkoxy, (lower)alkyleneoxy, phenyl, furyl, thienyl, di(lower)alkylamino, 1- piperidyl and ar(lower)alkyloxy.

As has been previously noted, compounds of the instant invention can form acid addition salts. Basic compounds of the present invention are converted to the acid addition salts by interaction of the base with an acid either in an aqueous or non-aqueous medium. In a similar manner, treatment of the acid addition salts with an aqueous base solution, e.g., alkali metal hydroxides, alkali metal carbonates and alkali metal bicarbonates or with a metal cation which forms an insoluble precipitate with the acid anion, results in a regeneration of the free base form. Such conversions are best carried out as rapidly as possible and under temperature conditions and method dictated by the stability of said basic products. The bases thus regenerated may be reconverted to the same or a different acid addition salt.

In the utilization of the chemotherapeutic activity of those compounds of the present invention which form salts, it is preferred, of course, to use phannaceuticallyacceptable salts. Although water-insolubility, high toxicity, or lack of crystalline nature may make some particular salt species unsuitable or less desirable for use as such in a given pharmaceutical application, the water insoluble or toxic salts can be converted to the corresponding pharmaceutically-acceptable bases by decomposition of the salt as described above, or alternately they can be converted to any desired pharmaceutically-acceptable acid-addition salt.

Examples of acids which provide pharmaceuticallyacceptable anions are hydrochloric, hydrobromic, hydroiodic, nitric, sulfuric, or sulfurous, phosphoric, acetic, lactic, citric, tartaric, succinic, maleic, and gluconic.

The terminal complication of thrombus formation in ischaemic heart disease, cerebral vascular disease, leg-vein thrombosis, pulmonary embolism and peripheral vascular disease is well documented in the medical literature, and has recently been reviewed by Mustard, et al., Pharm. Rev., 22, 97 (1970). The causal role of platelet aggregation in the formation of thrombi, which are masses of agglutinated platelets and leucocytes as distinguished from clots in which the elements of the blood are randomly distributed, has been postulated by many medical studies and has been reviewed by Mustard, et al. The compounds of the instant invention mediate their remarkable antithrombogenic activity through their ability to inhibit the aforementioned platelet aggregation.

As previously indicated, the 4-amino6-arylpyrimidines of the present invention are all readily adapted to therapeutic use as inhibitors of platelet aggregation. Typical member compounds of interest in this series include 4-diethylamino-6- p-methoxyphenyl) pyrimidine, 4-diethylamino-o-phenylpyrimidine,

4- ethyl-n-propylamino -6-phenylpyrimidine, 4-diethylamino-6- Z-thienyl pyrimidine, 4-diethylamino-6- m-dimethylaminophenyl pyrimidine, 4- [ethyl 2-hydroxyethyl amino] -6-phenylpyrimidine, 4-ethylamino-6-phenylpyrimidine and 4- 2,2,2-trifluoroethylamino -6-phenylpyrimidine.

In addition to their usefulness as inhibitors to platelet aggregation, several congeners of this series show outstanding potency as smooth muscle relaxants and in particular as bronchodilators. Compounds notable for this therapeutic usefulness include 4-diethylamino-6- (m-acetylaminophenyl -pyrimidine,

4-diethylamino-6- (m-isobutrylaminophenyl pyrimidine,

4-diethylamino-6- (m-propionylaminophenyl) pyrimidine,

4-di-n-propylamino-6- (macetylaminophenyl) pyrimidine and 4-diethylamino-6- (p-acetylaminophenyl pyrimidine.

The 4-amino-6-arylpyrimidines and the pharmaceutically acceptable salts thereof, which are useful as inhibitors of platelet aggregation and bronchodilators in mammals, may be administered either as individual therapeutic agents or as mixtures of therapeutic agents. They may be administered alone, but are generally administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice. For example, they may be combined with various pharmaceutically-acceptable inert carriers in the form of tablets, capsules, lozenges, troches, hard candies, powders, sprays, aqueous suspensions or solutions, injectable solutions, elixirs, syrups and the like. Such carriers include solid diluents, or filters, sterile aqueous media and various nontoxic organic solvents. Moreover, the oral pharmaceutical compositions of this invention may be suitably sweetened and flavored by means of various agents of the type commonly used for this purpose.

The particular carrier selected and the proportion of active ingredient to carrier are influenced by the solubility and chemical nature of the therapeutic compounds, the chosen route of administration and the needs of the standard pharmaceutical practice. For example, where those compounds are administered orally in tablet form, excipients such as lactose, sodium citrate, calcium carbonate and dicalcium phosphate may be used. Various disintegrants such as starch, alginic acids, and certain complex silicates, together with lubricating agents such as magnesium stearate, sodium lauryl sulphate and talc, may also be used in producing tablets for the oral administration of these compounds. For oral administration in capsule form, lactose and high molecular weight polyethylene glycols are among the preferred materials for use as pharmaceutically-acceptable carriers. Where aqueous suspensions are to be used for oral administration, the compounds of this invention may be combined with emulsifying or suspending agents. Diluents such as ethanol, propylene glycol, glycerine and their combinations may be employed as well as other materials.

For purposes of parenteral administration and inhalation, solutions or suspensions of the instant compounds in sesame or peanut oil or in aqueous propylene glycol solutions can be employed, as well as sterile aqueous solutions of the soluble acid addition salts described hereinafter. These particular solutions are especially suited for intramuscular and subcutaneous injection purposes. The aqueous solutions, including those of the acid addition salts dissolved in pure distilled water, are also useful for intravenous injection purposes provided that their pH is properly adjusted beforehand. Such solutions should also be suitably buffered, if necessary, and the liquid diluent first rendered isotonic with sufiicient saline or glucose.

The compounds may be administered to subjects suffering from bronchoconstriction by means of inhalators or other devices which permit the active compounds to come into direct contact with the constricted areas of the tissues of the subject. When administered by means of a spray formulated as a 1% solution, utilization several times a day is preferred.

It is necessary that the active ingredient form a proportion of the composition such that a suitable dosage form will be obtained. Obviously, several dosage unit forms may be administered at about the same time. Although compositions with less than 0.005% by weight of active ingredient might be used in certain instance, it is preferred to use compositions containing not less than 0.005% of the active ingredient; otherwise the amount of carrier becomes excessively large. Activity increases with the concentration of the active ingredient. The composition may contain 10, 50, 75, or an even higher percentage by weight of the active ingredient.

Although the use of the present invention is directed toward the treatment of mammals in general, the preferred subject is humans. In determining an efiicacious dose for human therapy, results of animal testing are frequently extrapolated and a correlation is assumed between animal test behavior and proposed human dosage. When a commercially employed standard is available, the dose level of the clinical candidate in humans is frequently determined by comparison of its performance with the standard in an animal test. For erample, theophylline is employed as a standard bronchodilator and is administered to humans at the rate of 150 to 300 mg. every 4 hours. It is assumed, then, that if compounds of the present invention have activity comparable to theophylline in the test assay, that similar doses will provide comparable responses in humans.

Obviously, the physician will ultimately determine the dosage which will be most suitable for a particular individual, and it will vary with the age, weight and response of the particular patient as well as with the nature and extent of the symptoms and the pharmacodynamic characteristics of the particular agent to be administered. Generally, small doses will be administered initially, with a gradual increase in the dosage until the optimum level is determined. It will often be found that when the composition is administered orally, larger quantities of the active ingredient will be required to produce the same level as produced by a small quantity administered parenterally.

Having full regard for the foregoing factors it is con sidered that an effective daily dosage of the compounds of the present invention in humans of approximately 100-1000 mg. per day, with a preferred range of about 150 to 600 mg. per day in single or divided doses, or at about 20 to 85 mg./kg. of body weight will elfectively prevent thrombus formation in human subjects prone to said disorder, and alleviate bronchoconstriction. These values are illustrative, and there may, of course, be individual cases where higher or lower dose ranges are merited.

The following examples are provided solely for the purpose of illustration and are not to be construed as limitations of this invention, many variations of which are possible without departing from the spirit or scope thereof.

EXAMPLE I 4-dimethylamino-6-phenylpyrimidine hydrochloride METHOD A (A) Ethyl Z-aminocinnamate (I; Ar=C H To a solution of dry ethyl ether (300 ml.) is added magnesium turnings (16.9 g.). Bromobenzene (103 g.) in ether (600 ml.) is added at a rate to maintain gentle refluxing. (An iodine crystal or a ml. of methyliodide often must be added to initiate the reaction.) Refluxing is continued until most of the magnesium has reacted. Ethyl cyanoacetate (30 g.) is added over a 30 minute period and the reaction mixture allowed to stir for 3 hours at room temperature after which time 3.5 N sulfuric acid (180 ml.) is added and the reactionv allowed to stir for 30 additional minutes. The aqueous layer is extracted with diethyl ether and the organic layer washed with water and dried over sodium sulfate. Removal of the ether in vacuo followed by distillation of the residual oil gives the desired product, B.P. at 0.4 mm., l38-142 C.

(B) 4-hydroxy-6-phenylpyrimidine (II; Ar=C H To a mixture of ethyl Z-aminocinnamate (54 g.; 0.28 mole) and formamide (100 ml.) in dimethylsulfoxide (700 ml.) at 100 C. is added via a dropping funnel potassium t-butoxide (63 g.; 0.56 mole) in 300 ml. of the same solvent over a minute period. The solution is stirred for 16 hours at 100 C. after which time it is cooled, poured over ice (2 l.) and acetic acid added to complete precipitation. The solid obtained upon filtration is washed with water, isopropyl alcohol and air dried, g., M.P. 266267 C.

(C) 4-chloro-6-phenylpyrimidine (III; Ar=C H 4-hydroxy-6-phenylpyrimidine (2.1 g.) is added to phosphorous oxychloride (60 ml.) and refluxed for 1.5 hours. Excess phosphorous oxychloride is removed in vacuo, and the dark oil poured over concentrated ammonium hydroxide/ice. The precipitate which forms is filtered, washed with water and dried, 2.1 g., M.P. 9598 C.

(D) 4-diethylamino-6-phenylpyrimidine hydrochloride 6 5; 1, 2= 2 5) A mixture of 4-chloro-6-phenylpyrimidine (10.0 g.), diethylamine (7.5 g.) and ethanol (200 ml.) is refluxed for 5 hours. At the end of this time the reaction mixture is poured into water (800 ml.) and extracted with chloroform. The chloroform layer is dried and concentrated in vacuo to an oil which is taken up in methanol, treated with activated charcoal, filtered and the methanol removed in vacuo. The residual oil is taken up in diethyl ether and anhydrous hydrochloric acid bubbled into the solution until precipitation is complete. Filtration yields the hydrochloride salt (6.45 g.) which is recrystallized from ethanol/hexane to yield a tan microcrystalline solid, 5.0 g., M.P. 214215 C.

Analysis.Calcd. for C H N -HCl (percent): C, 63.7; H, 6.9; N, 15.9. Found (percent): C, 63.6; H, 7.0; N, 15.7.

EXAMPLE II 4-diethylamino-6-phenylpyrimidine hydrochloride METHOD B (A) 2-carbomethoxy-3-aminobenzothiophene (V; X=H) To a solution of t-butyl alcohol (30 ml.) and potassium t-butoxide (1.12 g.; 0.01 mole) is added via a dropping funnel methyl thioglycolate (1.06 g.; 0.01 mole) in t-butyl alcohol (10 ml.). The solution is stirred for 10 minutes and then concentrated is vacuo to yield the sodium salt of methyl thioglycolate, which is taken up in 30 ml. of dimethylformamide. To this is added via a dropping funnel 2-chlorobenzonitrile (1.37 g.; 0.01 mole) in dimethylformamide (10 ml.), and the solution is warmed to C. for 30 minutes. At the end of this time the solution is cooled and poured onto 200 ml. of ice and water. The resultant precipitate is filtered, washed with water and dried to yield a white microcrystalline solid, 1.8 g., M.P. 105-106 C.

(B) 4-hydroxybenzothieno [3,2-d] pyrimidine (v1; X=H) To a solution of 2-carbomethoxy-3-aminobenzothiophene (2.07 g.; 0.02 mole) and potassium t-butoxide (2.24 g.; 0.02 mole) in dimethylsulfoxide (30 ml.) is added an excess of formamide (ca. 5 ml./g. of 2-carbomethoxy-3-aminobenzothiophene). This is heated to C. until the reaction is complete as evidenced by thin layer chromatography (-30 minutes). The solution is cooled, poured into water, acidified with glacial acetic acid and the resultant solid is filtered. Washing with isopropyl alcohol and then ether yields a white solid, 1.76 g., M.P. 300301 C.

(C) 4-chlorobenzothieno 3,2-d] pyrimidine A mixture of 4-hydroxybenzothieno[3,2-d1pyrimidine (20 g.; 0.1 mole) in phosphorous oxychloride (500 ml.) is refluxed with stirring for 4 hours. At the end of this time the solution is cooled and concentrated in vacuo to a brown semisolid, which is poured into 250 g. ice/250 ml. ammonium hydroxide solution. The resultant solid is filtered and air dried to yield a beige microcrystalline solid, 19.7 g., M.P. 139-140" C.

(D) 4-diethylaminohenzothieno[3,2-d]pyrimidine hydrochloride (VIII; X=H; R R =C H A mixture of 4-chlorobenzothieno[3,2-d1pyrimidine g.; 0.068 mole) and an excess of diethylamine in ethanol (500 ml.) is refluxed with stirring for 3 hours. The solution is cooled, poured into water (500 ml.) and extracted with chloroform. The chloroform extracts are washed with water, dried over sodium sulfate and the chloroform removed in vacuo to yield a dark oily residue. This is taken up in methanol, treated with activated charcoal, filtered, and the solvent removed in vacuo to yield an oily residue which is taken up in diethyl ether. Anhydrous hydrogen chloride gas is bubbled into this solution until precipitation ceases. Filtration yields the hydrochloride salt, 13.4 g., M.P. 226-230 C.

(E) 4-diethylamino-6-phenylpyrimidine hydrochloride 1 F z s) To a. solution of 1.5 ml. of dimethylformamide containing 4-diethylaminobenzothieno[3,2-d]pyrimidine (2.0 g.) is added a large excess of Raney nickel and the resulting mixture heated to reflux. Water is allowed to distill from the reaction mixture until the temperature reaches 150 C. where refluxing is continued with rapid stirring for 48 hours. The solids are filtered and the filtrate con centrated in vacuo to an oil. The residual oil is partitioned between Water and chloroform and the organic layer separated and dried over sodium sulfate. Removal of the solvent under reduced pressure provides an oil which when dissolved in ethyl ether and treated with gaseous hydrogen chloride provides 1.4 g. of the hydrochloride salt of the desired product, which is identical in every respect to that synthesized via Method A.

EXAMPLE HI 4-diethylamino-6-phenylpyrimidine hydrochloride METHOD C (A) 4-hydroxy-2-mercapto-6-phenylpyrimidine B 5) A 50 gal. reaction vessel is charged with 110.01. of dry ethanol, 10.24 kg. (53.4 moles) of ethyl benzoylacetate, 5.78 kg. (106.8 moles) of sodium methoxide and 7.25 kg. (95.2 moles) of thiourea. The reaction mixture is heated to the reflux temperature (79 C.) and stirred at that point for 120 hours. During this contact period a clear solution is obtained and then crystalline material gradually starts to precipitate. The resulting slurry is concentrated in vacuo to a low volume and the concentrate then diluted with 40 l. of water. A second concentration of the aqueous mixture is carried out in vacuo to give a thick slurry, free of ethanol, which is taken up in 120 l. of water. The aqueous solution is chilled to 10 C. and then acidified to pH 3.0 by the slow addition of concentrated hydrochloric acid. The crystalline slurry is granulated for 30 minutes at C. and then filtered. The cake is Washed with Warm water (60 l. at 35 C.) and then dried at 60 C. in a steam oven for 48 hours. The yield of dry material is 7.82 kg., M.P. 258262 C. (decomposition).

(B) 4-hydroxy-6-phenylpyrimidine (II; Ar=C H A 50 gal. reaction vessel is charged with 7.68 kg. (37.6 moles) of 2-mercapto-4-hydroxy-6-phenylpyrimidine, 75.0 1. of water and 3.0 kg. (75.0 moles) of sodium hydroxide pellets. The solution is stirred at 65 C. as 66.0 kg. of Raney nickel sludge is added portionwise over a 30 minute period. The aqueous slurry is then stirred at 85 C. for one hour. An additional 7 kg. of Raney nickel sludge is added and the slurry stirred at 85 C. for another 30 minutes to complete the desulfurization. The reaction mixture is cooled to 30 C., filtered and the nickel cake washed with a solution of 1.2 kg. sodium hydroxide in 40 l. of water. Acidification of the clear filtrate to pH 4.7 with concentrated hydrochloric acid gives a crystalline product that is collected. The cake is washed with 20 1. of water and dried at 60 C. for 48 hours to give 5.84 kg. of product, M.P. 272278 C. (decomposition).

(C) 4-chloro-6-phenylpyrimidine (III; Ar=C H A slurry of 5.8 kg. (33.7 moles) of 4-hydroxy-6-phenylpyrimidine in 30.0 1. of phosphorous oxychloride is stirred and heated to the reflux temperature (-1 10 C.). At 78 C. all of the solid materials are dissolved, and the solution then is stirred at C. for 5 hours. The solution is concentrated in vacuo to a volume of ca. 10 liters, and then carefully added at 50 C. to a mixture of 60.0 1. concentrated ammonium hydroxide, lbs. of ice and 40 l. of chloroform. The addition of the warm reaction mixture requires about 10 minutes and the final temperature is 10 C. The resulting mixture is stirred for 15 minutes and the layers then are separated. The aqueous phase is extracted twice with 20 1. portions of chloroform and the extracts combined. The extracts are backwashed twice with 80 1. portions of water, dried over anhydrous magnesium sulfate and treated with Darco KB. Concentration of the clear chloroform solution to a volume of ca. 12 1. followed by the addition of 12 l. of hexane gives a crystalline slurry. The slurry is concentrated in vacuo to a final volume of about 15 liters and then filtered. The cake is washed with hexane and dried in the atmosphere to give 5.25 kg. of product, M.P. 101-105 C.

(D) 4-diethylamino-6-phenylpyrimidine (IV; Ar=C H A 22 1. round bottom flask is charged with 11.0 1. of anhydrous ethanol, 1.24 kg. (6.52 moles) of 4-chloro-6- phenylpyrimidine and 1.43 kg. (19.56 moles) of anhydrous diethylamine. The reaction solution is then stirred at the reflux temperature (80 C.) for 5 hours. When completion of reaction is assured the solution is concentrated in vacuo to a thick slurry. The concentrate is diluted with 12.0 1. of chloroform and chilled to 15 C. in an ice bath. Four liters of cold 10% aqueous sodium hydroxide solution is added and the mixture stirred 10 minutes at 10-15 C. The layers are separated and the organic phase washed twice with 4 1. portions of water. The chloroform solution is dried over anhydrous magnesium sulfate, treated with Darco KB and concentrated in vacuo to an oil. The oil is taken up in 41. of fresh chloroform and the solution reconcentrated. Reconstitution of the concentrate with 9 l. of chloroform gives a solution which is chilled to 10 C. and then stirred as 255.0 g. (7.0 moles) of anhydrous hydrogen chloride is added beneath the surface. The acidified solution is concentrated in vacuo to a volume of 5 liters (slurry). The slurry is then distilled at atmospheric pressure as acetone is continuously added. When most of the chloroform is gone the slurry is made up to a 9 1. volume with acetone, chilled to 20 C. and filtered. The cake is washed with acetone and dried at 60 C. in a steam oven to give 1.64 kg. of crude product, M.P. 2182l9'.5 C.

The crude product is taken up in a mixture of 15.0 1. of methylene chloride and 1.0 l. of chloroform at 45 C. and filtered. The clear solution is distilled at atmospheric pressure as acetone is continuously added. When most of the methylene chloride is gone the acetone slurry (9' l.) is cooled to 20 C. and filtered. The cake is washed with acetone and dried in a steam oven at 75 C. for 4 hours. The yield is 1.61 kg., M.P. 218219 C.

EXAMPLE IV The procedures of Example I are repeated, using the appropriately substituted starting materials, to provide the following compounds in good yields:

R1 R2 M.P., C

H CH3 218-220 H CZHG 190-192 H I1-C3H7 172-174 H 1-C3H7 165-167 H H-CqHo 142-145 H i-C Hg 138-140 H H 207-209 CH3 CHa 250-252 CH3 11-03117 172-174 C2H6 C2115 173-175 02115 11-C H7 187-188 11-03117 n-CaH'! 152-154 I1-C4Hp 11-04119 90-91 1-C4H9 PC4119 103-104 EXAMPLE V Following the procedures of Example II, and starting with the requisite benzothieno[3,2-d]pyrimidine the following products are prepared in moderately good yields:

4 (l-pyrrolidinyl)-6-phenylpyrimidine hydrochloride,

M.P. 266-268 C.;

4-(l-piperidyl)-6-phenylpyrimidine hydrochloride, M.P.

4-(l-hexahydroazepinyl)-6-phenylpyrimidine hydrochloride, M.P. 65 C.;

4 (4-morpholinyl)-6-phenylpyrimidine hydrochloride,

M.P. 259-260 C.;

4 (4-methyl-l-piperazinyl)-6-phenylpyrimidine dihydrochloride, M.P. 290292 C. (decomposition).

EXAMPLE VI Again, employing the procedures of Example I, and utilizing the appropriate starting reagents, the following congeners are prepared:

EXAMPLE VII Utilizing the procedure of Example I-D, and employing 4-chloro-6-phenylpyrimidine and the appropriate amine, the following congeners are synthesized:

EXAMPLE VIII The procedures of Example II are repeated, starting with the appropriately substituted benzothieno[3,2-d]pyrimidine, to provide the following analogs:

NW O

R R2 R1 R:

H Z-pyrldylmethyl. H 2-sulIam0ylphenyL CH3 Z-pyridylmethyl. CH3 2-suliamoy1phenyl. n-C H 2-pyrldylrnethyl. n-C H 2-sulfamoylphenyl. H 3-pyridylmethyl. H Z-carboxyphenyl. CH3 3-pyridylmethyl. CH3 Z-carboxyphenyl. CH3 4-pyridylmethyl. i-C H1 2carboxyphenyl.

EXAMPLE IX Following the procedures of Example I, and starting with the appropriate reagents, the following compounds are synthesized:

4-diethylamino-6- m-chlorophenyl) pyrimidine hydrochloride, M.P. 178180 C.; I

4-diethylamino-6- (p-chlorophenyDpyrimidine hydrochloride, M.P. 2l5-216 C.;

4-di (n-propyl) amino-6- (p-chlorophenyl pyrimidine hydrochloride, M.P. 157-158" C.;

4-dimethylamino-6- (p-chlorophenyl) pyrimidine hydrochloride, M.P. 268-270" C.;

4-( l-pyrrolidinyl) -6- (p-chlorophenyl) pyrimidine hydrochloride, M.P. 265-2-67 C.;

4-(4-methyl-l-piperazinyl)-6-(p-chloropheny1)pyrimidine hydrochloride, M.P. 295 C.;

1 7 4-[methyl(2-hydroxyethyl)amino] -6-(p-chlorophenyl) pyrimidine hydrochloride, M.P. 203-205 C.; 4- (2,2,2-trifiuoroethylamino)=6-(p-chlorophenyl)pyrimidine hydrochloride, M.P. 227-229 C.; 4-di (n-propyl amino-6- m-trifluoromethylphenyl pyrimidine hydrochloride, M.P. 276-278 C.

EXAMPLE X Again, following the procedures of Example I, and starting with the appropriately substituted reagents, the following analogs are prepared in moderate yields:

Repeating again the procedures of Example I, and employing the proper starting reagents, the following 6-(pmethoxyphenyl) pyrimidine hydrochlorides are synthesized:

\ Decomposition. 1 Dihydrochloride (decomposition).

18 EXAMPLE XII Following the experimental details of Example I, and starting with the appropriately substituted reagents, the

following compounds are prepared:

EXAMPLE XIII 4-diethylamino-6-(p-hydroxyphenyl)pyrimidine hydrobromide A solution of 18.6 g. (0.1 mole) of 4-diethylamino-6-(pmethoxyphenyDpyrimidine in 30 ml. of 48% hydrobromic acid and 30 ml. of glacial acetic acid is heated to the reflux temperature and gaseous hydrogen bromide slowly introduced below the surface during the first two hours of refluxing. Heating is continued until thin layer chromatography indicates the reaction is complete. The reaction is cooled and the excess acetic acid and hydrobromic acid are removed under reduced pressure. The residual product is triturated with acetone, filtered and recrystalllized from ethanol/ hexane.

EXAMPLE XIV Following the procedure of Example XIII and starting with the 6-(methoxyphenyDpyrimidines of Example XII and the appropriate reagents the following analogs are prepared:

19 EXAMPLE XV The method of Example III is repeated, using the requisite starting reagents, to provide the following congeners in moderate yields:

EXAMPLE XVI 4-diethylamino-6-(m-nitrophenyl)pyrimidine hydrochloride To a solution of 1.0 g. (3.8 mmoles) of 4-diethylamino- 6-phenylpyrimidine hydrochloride in 10 ml. of concentrated sulfuric acid is added 10 ml. of nitric acid dropwise at room temperature. The reaction mixture is allowed to stir for 6 hours, and is then poured onto ice and made basic with concentrated ammonium hydroxide. The product is extracted into chloroform, and the organic layer dried over sodium sulfate and concentrated in vacuo to an oil. The residual oil is dissolved in ethyl acetate and hydrogen chloride slowly introduced into the solution until the precipitation is complete. The hydrochloride salt is filtered, dried and recrystallized, mp. 238-240 C.

Analysis.Calcd. for C H O N -HCl (percent): C, 54.5; H, 5:6; N, 18.2. Found (percent): C, 54.1; H, 5.6; N, 18.0.

EXAMPLE XVII The nitration procedure of Example XVI is repeated, using the appropriate starting reagents, to provide the following analogs in good yields:

20 EXAMPLE XVIII The procedure of Example II is repeated, starting with the appropriate bnezothieno[3,2-d1pyrimidine, to provide in moderate yields the following compounds:

EXAMPLE XIX 4-diethylamino-6- (m-aminophenyl) pyrimidine dihydrochloride A solution of 24.5 g. (0.8 mole) of 4-diethylamino-6- (m-nitrophenyl)-pyrimidine hydrochloride, 62 g. of stannous chloride and 370 ml. of 12 N hydrochloric acid contained in a 2 l. 3-necked flask is heated and stirred for 3 hours at C. and then allowed to stir at room temperature overnight. The precipitate is filtered, washed with 12 N hydrochloric acid and dissolved in water. The aqueous solution is made basic with 10% sodium hydroxide solution and extracted with chloroform. Separation of the organic layer followed by drying over sodium-sulfate and concentration to dryness provides the crude product as an oil. The residue is redissolved in chloroform and treated with gaseous hydrogen chloride until a precipitate no longer forms. The product is filtered and dried, 19.1 g., M.P. 245-247 C.

M01 wt.: Calcd. for 3l5.25. Found: 311. Equiv. wt.: Calcd. for 157.62. Found: 161.

The free base, generated by treating an aqueous solution of the hydrochloride salt with a 10% sodium hydroxide solution, has a melting point of 78 C.

Analysis.Calcd. for C I-I N. (percent): C, 69.4; H, 7.5; N, 23.1. Found (percent): C, 69.0; H, 7.5; N, 23.2.

EXAMPLE XX The procedure of Example XIX is repeated, starting with the compounds of Examples XVII and XVIII, to synthesize the following congeners:

60 HzN R R7 R1 R2 1 2 65 R:

NH2position of H C2115 CFaCHz H H L a OFKOHZ 02H substitution R R: H n-CiH H Ha)2N( 2)I- 2 H H CH; CH3 CH3 2 2- 2 OH; H CH; n-CaH7 CzHs HO( H2 2- CzH5 CgHs n-C3H1 CH3 YCIO CeHu HO(CH2)zn-CzH1 n-CaH1 2)2- W K B CzHs (CHg) HO(CHz)z- HO(CH2)Z C H (CHz)5 CHz- CHCH; CH2=CHCHz C 11 (CH2 a- H 2-HO2CCeH4 -0 11, -(CH2) z0( H2)2 H 2-HzNSOzCoH H -(CH2) 2N(CH3) (CH2)2 lit-C411 11-04119 TABLECntinued EXAMPLE XXI 4-diethylamino-6-(m-acetylaminophenyl pyrimidine hydrochloride Acid chloride method.--To a suspension of 2.3 g. of sodium carbonate in 140 ml. of ether containing 5.1 g. (0.021 mole) of 4-diethylamino-6-(m-aminophenyl)pyrimidine is slowly added 1.6 g. of acetyl chloride in 20 ml. of the same solvent. The reaction mixture is stirred for 24 hours and is then treated with water. The ether layer is separated, dried over sodium sulfate and concentrated in vacuo to an oil, which is taken up in ethyl acetate and treated with gaseous hydrogen chloride until a precipitate no longer forms. The product is filtered and recrystallized from ethyl acetate/methanol, 2.1 g., M.P. 236238 C.

Analysis-Calm. for C H ON -HCl (percent): C, 54.5; H, 5.6; N, 17.9. Found (percent): C, 54.1; H, 5.6: N, 18.0.

Anhydride method.-To 5.6 g. (0.022 mole) of 4-diethylarnino-6-(m-aminophenyl)pyrimidine is slowly added, with cooling, 25 ml. of acetic anhydride. The resulting solution is stirred overnight at room temperature and is then diluted with 500 ml. of ethyl acetate and treated with sufficient gaseous hydrogen chloride to complete the precipitation of the desired product. The solvent and excess acetic anhydride are removed under reduced pressure and the residue washed from the flask with 20 ml. of 1:1 hexane/ethyl acetate 6.6 g., M.P. 235237 C. It proves to be identical to that prepared by the Acid Chloride Method.

EXAMPLE XXII Starting with the suitably substituted G-aminophenylpyrimidine and requisite reagents and following the appropriate procedure method in Example )QCI the following compounds are prepared:

Method X R1 R2 C Anhydride 3-NHC OCH3 n-CaH1 n-CaH 128-129 D0- 3-NHCOCH3 (CH2)4- 289-291 D0 3-NHCOCH3 n-C-iHn n-CrHg 193-195 Acid chlon 3-NHC O CzHs 2H5 2H5 232-234 D0"... 3-NHCO(CH2)zCH3 C2115 C2H5 215-218 DO 3-NHCOCH(CH3)2 2H5 CgHs 248250 D0 3-NHCOCF3 2H5 2H5 149-151 D0 3-NHCOC6H5 C2115 CgHs 230-234 DO- 3-NHCO2CH3 C2115 C2115 1 223 D0 3NHCOzCzH5 02H; C H 1 224 D0. 3-NHSOzCH3 CzH5 C2115 225 DO 3-NHSO2CH3 n-C3H7 Il-C3H1 205 Anhydrlde 4-NHCOCH3 CJHS C 115 272-275 Decomposition.

22 EXAMPLE XXIII The procedure of Example XXI is repeated, using the appropriate starting materials, to provide the following analogs:

Method X R; R2

2-NHCOCH3 C2H5 C2115 D0 2-NHCOCH3 C2115 H-C3H7 DO 2-NHCO (CH2) zCHa C H-C3H7 D0 2-NHCO CH(CH )2 C2H5 C2115 Acid chloride"... 2-NHS02CH3 2H5 C2H5 Do 3-NHSOzCsH5 H: CH3 D0 3-NHCOCHzCHa -(CH2)5 Anhydride 3-NHCOCH3 H 2-HO2CC5H4 D0. 3-NHCOCH3 H 2-H2NSO2C5H4 D0--- 4-NHCOCH3 CH3 CH3 DO... 4-NHCOCH2CH3 CH3 CH Acid chl0ride 4-NHCO CH(CH 2 CH CH Anhydride 4-NHCOCH n-C3H7 n-C3H D0 l-NHCHO I1-C3H7 I1-C3H7 Acid chloride. 4-NHSO CH3 CH3 CH3 D0 4-NHCOgCzH5 CH3 CH3 D0 4-NHCOC5H5 11-C3H1 n-C3H1 EXAMPLE XXIV 4-diethylamino-6- (m-dimethylaminophenyl) pyrimidine hydrochloride To a solution of 2.6 g. (9.3 mmoles) of 4-diethylamino 6 (m-aminophenyl) pyrimidine hydrochloride in 50 ml. of water is added 4.72 g. of sodium carbonate followed by. the slow addition of 2.74 g. of methyl iodide. The reaction mixture is heated to the reflux temperature for 6 hours, and is then cooled and extracted with chloroform. The organic layer is separated, dried over sodium sulfate and evaporated in vacuo to a light brown oil. Chromatographing on a silica gel column and eluting with ethyl acetate provides the desired product as a light yellow oil which when dissolved in ethyl acetate and treated with gaseous hydrogen chloride provides the corresponding crude hydrochloride salt. Further purification is eflected by recrystallization from methanol/ethyl acetate, 0.9 g., M.P. -173 C.

EXAMPLE XXV Following the procedure of Example XXIV, and starting with the requisite 6-aminophenylpyrimidine and appropriate reagents, the following compounds are syn- EXAMPLE XXVI Starting with 2-bromothiophene and the requisite reagents, and following the procedure of Example I, the following congeners are prepared:

R1 R2 M.P., C

H H 204-205 CH3 H 238-240 C2115 H 208-210 CF3CH2 H 110 CH3 CH3 256-257 CzHs CzHs 153-155 CFZCHZ CzHis 158-161 a n-CaH1 47-148 CH2=0HCH2 CHz= CHCH: 151-152 CH HO (CHz)z- 196-198 C2115 HO(CH2)2- 175476 HO(CH2)2 HO(CHz)z- 175-177 EXAMPLE XXVII 4-diethylamino-6-(S-acetylamino-Z-thienyl) pyrimidine hydrochloride A mixture of 28.26 g. (0.09 mole) of 4-diethylamino- 6-(5-nitro-2-thienyl)pyrimidine hydrochloride and 35 g. of. granular tin is treated, portionwise, with 75 ml. of concentrated hydrochloric acid. Cooling is necessary once the reaction has started. When the reaction has subsided, the clear hot solution is decanted from the unreacted tin and cooled in a salt-ice bath, and the resulting amine hydrochloride-stannic chloride complex which precipitates is filtered.

The complex is added to 75 ml. of water and 80 ml. of diethyl ether, and treated with sufiicient sodium hydroxide to provide a pH of 9-10. The ether layer is separated, treated with 14.8 g. (0.135 mole) of acetic anhydride and heated to reflux for 3 hours. The resulting solution is washed with sodium hydroxide solution, separated, dried over sodium sulfate and concentrated to dryness. The product is dissolved in ethyl acetate and sufficient hydrogen chloride gas bubbled into the solution to precipitate the product as the hydrochloride salt. Recrystallization from isopropanol provides the pure product.

EXAMPLE XXVIII Employing the procedure of Example XXV II, and starting with the appropriate reagents, the following compounds are synthesized:

4-3 RCONH I 24 EXAMPLE XXIX The procedure of Example III is repeated, starting with the appropriate reagents, to provide the following congeners in good yields:

Position of substitution R1 EXAMPLE XXX The procedure of Example III is again repeated, using the requisite starting reagents, to provide, in good yields, the following products:

EXAMPLE XXXI The procedure of Example I is repeated, starting with the appropriate 2- or 3-halobenzo[b]thiophene and requisite reagents, to provide the following compounds in moderately good yields:

EXAMPLE XXXII 4-diethylamino-6-(S-acetylamino-Z-furyl)pyrimidine hydrochloride To a mixture of 2.62 g. (0.01 mole) of 4-diethylamino- 6-(5-nitro-2-furyl)pyrimidine and aluminum amalgam, prepared from 4.0 g. of aluminum turnings, in 60 ml. of diethyl ether is added 4 ml. of water. Acetic anhydride (2.0 g.; 0.02 mole) is added dropwise during the ensuing reaction which is maintained by heating the reaction vessel in a warm water bath. The ether is filtered and the filtrate dried over sodium sulfate. Removal of the solvent under reduced pressure provides the crude product. The residue is dissolved in ethyl acetate and treated with gaseous hydrogen chloride until a precipitate no longer forms. The resulting hydrochloride salt is further purified by several recrystallizations from methanol/hexane.

EXAMPLE XXXIII The reduction-acylation procedure of Example XXXII is repeated, using the appropriately substituted starting materials, to provide the following analogs:

26 EXAMPLE XXXIV The procedures of Examples XIX and XXI are repeated, using the requisite starting reagents, to provide the following compounds in moderate yields:

R C ONE- 2 N N 1 I N N R R1 Position of substitution RCONH Pyridyl R R R2 3. 2 CH CH CH 4. 2 CH: CzHi C2Hs 4. 2 0 115 (32H; CzH5 4..-. 2 CH3 CFzCHz 02H:, 5. 2 CH3 2H5 C2115 4. 3 CH3 02H; 02H; 5. 3 CH3 02H; 02H; 35 5. 3 2 2)5 5. 3 CH3 CFzCHg 02135 6.... 3 CH: H3 Cyclo 05H 2.-.. 4 CH CqHs C2H5 2.. 4 I1-C4H9 CH3 CH1 2, 4 l-C3H1 C 115 2 :5 2. 4 CH3 CFgCH: 05115 3. 4 CH: 2) Z (CH2)I 4O 3.. 4 C311 02H; C2H5 3 4 CzH; CzHi EXAMPLE XXXV 4-diethylamino- 6- (2-fu ryl pyrimidine hydrochloride Crude 4 diethylamino 6-(2-furyl)pyrimidine (3.2 g.; 0.015 mole), obtained by repeating the procedures of Example III, is dissolved in 25 ml. of dry ethyl acetate and treated with 1.44 g. (0.016 mole) of oxalic acid. The resulting solution is warmed briefly on a steam bath, and is then cooled in a salt-ice bath. The resulting oxalate salt is filtered, dried and recrystallized from methanol/hexane. The purified oxalate is dissolved in a minimum amount of Water and the pH adjusted to 9 using a 5% sodium hydroxide solution. Ethyl acetate is added and the free base rapidly extracted. The organic phase is dried over sodium sulfate and treated with suflicient gaseous hydrogen chloride to completely precipitate the hydrochloride salt, which is filtered, washed with acetone and dried, M.P.

EXAMPLE XXXVI Starting with the appropriately substituted reagents and employing the respective procedures indicated, the following products are synthesized:

Analysis.--Calcd. for C H ON (percent): 0, 69.8; H, 6.4; N, 19.4. Found (percent): C, 69.8; H, 6.5; N, 19.6.

EXAMPLE XXXVIII \'-R| X: Rl\I/ R1 R2 X1 X: R: R: R; R; Procedure a-omoo H CH; OH; H H Example III. a-omco H 02H8 0211; H H Do. 3-CHsC0 H (CHz)s H H Do. 4-GHJCO H CFaCHz C2Hs OH: H Do. 4-CH;C0 H HO(CH2)r- (EH5 CH: H Do. 44313.00 H H HOzCCuH| CH; H Do. L-CHzCO H -(CHz)4- OH; H Do.

3,4-CH201 C2Hs CH5 H H Example I. 3,4-CH3O: HO(CH2)z' 02H. H H D0. 3,4-CHzO: CHaCHa 2H5 H H D0. 3,4-CH20z CHFCHCH: CzHs H H D0. S-NO: C2Hs 2115 H H Example XVI. 3-N0, 4-Cl CFaCH: 02115 H H D0. 3-NO3 4'0CHQ CFaCH: 02115 H H D0. s-Nol 4-0OH= CzHs (EH5 H H Do. S-NO: 4-F (CH2)s- H H D0. 3-NH2 4-01 02H! 02115 H H Example. XIX. 3-NH1 4-01 CFzCHa 02115 H H Do. a-NH: 4-OCH3 CFzCHz 02H; H H Do. a-NH: 4-0011: 02H; CzH5 H H D0. S-NH: 4-15 -(CH)5 H H Do. 3-CHICONH 4-01 (EH5 02H: H H Example XXI. 3-CH3CONH 4-01 CFaCHz CzHn H H Do. S-OHzCONH 4-0011; CFQCH: 02H: H H Do. a-omcoNH 4-OCH; 0 H; 02H; H H Do. 3-CHCONH 4-F --(CH2)5- H H D0. B-CHsOzCNH 4-01 02H; 02H. H H Do. 3-C2H502CNH 4-OCHI CzHs CzHn H H D0. 3-CgH50zCNH 4-F (CHz)5- H H Do. H H C2H5 CzHs CH: H Example I H H HO(CH2)2- 02H: OH; H Do. H H CFQCFZ CzHa OH; H D0. 3-CH3CONH H 2H5 2H& CH: CH: D0. 3-CH3CONH H CzHs CFQCHZ CH3 CH3 D0. 3-CH1CONH H 02H C2115 H 02H; D0. 3-CH3C0NH H CzHs 02H: 02H: H D0. a-(oHmNco H 02H. 02H; H H Example XXI. 3-(C:H5)NCO H 02H; 02H; H H Do.

EXAMPLE XXXVII TABLE- continued 1-[3-(6-d1ethylam1no-4-pyr1m1d1nyl)phenyl1-3- 40 phenylurea hydrochloride 3-q5NHCO OFgCH 02H. U B-CHzNHGO CF CHz 01H; To 2.6 g. (0.011 mole) of 4-d1ethylam1no-6-(m-ammofi-CIl-IIfiNCEgCO 8g; 8g: phenyl)pyr1m1d1ne m 40 ml. of ether is added dropwise 1.3 g. of phenyhsocyanate dissolved in 40 ml. of the same 4-CHaNHC0 3 1 a 1 1 t d th lt' t 11 dt tir ht *CQHWHOO so ven an e resu mg mix ure a owe o s overmg 4 NHCO 33H, E0311, at room temperature. Removal of the solvent under reduced pressure provides the crude product, 3.4 g., whlch EXAMPLE XXXIX 1s recrystalllzed from ethyl acetate/methanol, 2.3 g., M.P. 183184 C Tablets A tablet base is prepared by blending the following ingredients in the proportion by weight indicated:

Sucrose, U.S.P. 80.3 Tapioca starch 13.2 Magnesium stearate 6.5

Capsules A blend is prepared containing the following ingredients:

Calcium carbonate, U.S.P. 17.6 Dicalcium phosphate 18.8 Magnesium trisilicate, U.S.P. 5.2 Lactose, U.S.P. 5.2 Potato starch 5.2 Magnesium stearate A 0.8

Magnesium stearate B 0.35

29 To this blend is added sufficient 4-diethylamino-6-(mdimethylaminophenyl)pyrimidine hydrochloride to provide capsules containing 20, 100 and 250 mg. of active ingredient per capsule. The compositions are filled into 30 EXAMPLE XLIlI Solution A solution of 4-diethylamino 6 (p-methoxyphenyl) pyrimidine hydrochloride is prepared with the following conventional 1hard gelatin capsules in the amount of 350 composition:

r mg p6 capsu 6 EXAMPLE XLI Effective ingredient 30.22 grams. Magnesium chloride hexahydrate 12.36 grams. Monoethanolamine 8.85 ml. lniectable preparatlon Propylene glycol 376.00 grams Water, distilled 94.00 ml.

one thousand grams Of 4-diethylamino-6-phenylpyrimi- The resultant solution has a concentration of effective dine hydrochloride are intimately mixed and ground with ingredient of 50 rug/ml. and is suitable for parenteral 2500 grams f Sodium ascorbate. The ground dry mixture and especially for intramuscular administration. is placed in vials and sterilized with ethylene oxide after EXAMPLE XLIV which the vials aresterilely stoppered. For intravenous ad- Starting with the appropriately substituted mimstration, sufficient water is added to the materials in arylpyl-imidine and requisite piperazine and repeating the the vials to form a solution containing 10 mg. of active procedure f Example 1 D, h following analogs are preingredient per milliliter of injectable solution. pared in good yields:

Ar N\I lg. N

i o x Ar X Ar X 05H; CH3 4-FC5H4 ocmomn CoHs OH(CH:)1 4-FCiH4 CH; C0115 OCH; 4-FC6H 2-furyl 4-C1CiH4 02H: 3-BrC|H4 2-furyl 4-C1C5H4 OCzHs 3-BlCnH4 C7H5 4-C1COH4 (H; (i-BIC H OCHzC CH3 =CHg 4-OCHaCuH4 OCHzCeHl 3-N (CHa):CoH4 OCH2C(CH1)=CH2 4-0 CHaCaH CHa 3-N (CH3)2CH| 2-furyl 4-OCHICuI-IA 2-tury1 3-N(CHa)2CoH4 2-tl11enyl 3-C1C9H4 OCHzC(CHa)=CHa 3-NHCOCH3COH4 OCzH5 a-oloirn oomowm 3-NHCOCH3CH4 can. 3-ClCsH4 2-thienyl 3-NHCOCHaCoHa l-plperidyl 4-CHIC6H4 Z-thlenyl 3-NHCOCH3C4H4 001120.11. 4-CH3C6H4 l-piperidyl 4-CH3C5H4 N(CHa)2 EXAMPLE XLII EXAMPLE XLV Suspension In vitro inhibition of platelet aggregation A suspension of 4-diethylamino-6-(m-propionylamino- The ability of the compounds of the present invention phenyl) pyrimidine is prepared with the following comto inhibit platelet aggregation in vitro is measured accordposition: ing to the method of Born, et al., J. PhysioL, 168, 178

(1963) and comprises the following procedure: gg g gi gg fi gi Anesthetized male rabbits are bled from a carotid G1 a U S P 18535 artery into plastic centrifuge tubes containing 0.1 volume G g 5 6 h 3% sodium citrate. Platelet-rich plasma is separated by g i anolidgne 0 d centrifugation at 100 G. for 10 minutes at 20 C. Plasma 3 35 alter i to make 1 liter from 3 animals is pooled; 5 ml. samples are placed into 1 clear plastic curvettes and stirred at 1000 r.p.m., followed To this suspension, various sweeteners and fiavorants by the addition of compounds of the present invention at are added to improve the palatability of the suspension. levels of 6x10- l0" and 10- moles/liter. After 10 The suspension contains approximately 25 mg. of effective minutes of incubation with the platelet-rich plasma at agent per milliliter. room temperature, collagen, a protein known to cause 31 platelet aggregation, is added (0.27 ml. collagen/4 ml. plasma) and changes in the optical density are followed with a Spectronic 20 colorimeter attached to a Houston Instrument TY Recorder. Platelet aggregation is indicated by a decrease in optical density. The relative potency of 5 the compounds of the present invention are thus rated on their ability to inhibit (percent) collagen induced platelet aggregation.

The following compounds were evaluated:

EXAMPLE XLVI 7 In vivo inhibition of platelet aggregation The capacity of the compounds of the present invention to inhibit platelet aggregation in a modified in vivo test is measured by the following procedure:

suspension per 20 ml. of platelet-rich plasma (high dose), and the second, a 1:4()50 dilution (low dose). Changes in optical density are then followed with a Spectronic 20 colorimeter attached to a Houston Instrument TY Recorder. Platelet aggregation is indicated by a decrease in optical density. The degree of inhibition of collagen induced ag- 33 gregation is reported as complete (95l00% partial (15- 95%) and none (-15 Measurements are carried out on the hourly samples, allowing for the determination of a duration of the initial effect.

Employing the above described procedure the following compounds were tested:

Ar= e s; 2= 02135 25 R0. Complete Complete AI=4-CHaO 05114; R], R2=C H EXAMPLE XLVII Bronchodilator activity Conscious female guinea pigs, which have been fasted for 12 hours, receive oral or parenteral dosages of the compound which is to be tested for effectiveness. Control animals receive doses of saline solution which do not contain the compound which is under test. Subsequent to this administration, each animal is challenged with histamine aerosol.

The challenge procedure consists of spraying a 0.4 percent aqueous solution of histamine, at a pressure of 5 lb./ in. into an 8 x 8 x 12 inch plastic container for one minute. Immediately after the container is subjected to histamine spray the animal is placed within it. At the end of one minute of exposure, the respiratory status, which is a reflection of bronchoconstriction, is evaluated. Evaluation levels are designated and scored as normal breathing (0), slightly deepened breathing (1), labored breathing (2), severely labored breathing and ataxis (3) and unconsciousness (4). Each group of animals contains 8 to 10 individuals and a control group containing the same approximate number is used. The scores for the control group and the group which has been treated with the compound under test are compared and the diiference is expressed as percent protection.

The dose, which is given orally, is 60 mg./kg. and the animals are challenged with histamine 60 minutes later. The standard compound used is theophylline, which gives 25' percent protection when a dose of 60 mg./ kg. is administered orally and the animal is challenged one hour later. When the compounds listed below are administered according to this procedure and the animals are challenged accordingly, the following percent protection is observed.

N Ar 1 Percent Ar R1 R2 protection 3-NO2C6H4 C2115 (32H; 20 3-CH CONHC6H4 C2H5 02115 40 3-CH3CONHC H -!1C3H1 I1-C3H1 3U 3-C2H5CONHC5H4 C2115 02115 30 3'(CH3)2CHCONHCQH| CzHs CzHs 22 4-CH CONHCaHg CgHs C2115 55 3-CH SOgNHCeH C2115 C2H5 19 2-furyl CzHs 02115 15 EXAMPLE XLVIII In vitro inhibition of platelet aggregation in human plasma The procedure of Example XLV is repeated except that platelet-rich plasma from nine human volunteers is employed in place of rabbit plasma. 4-(Diethylamino)-6- phenylpyrimidine hydrochloride provides the following inhibition (percent) of collagen induced platelet aggregation at the indicated concentrations:

Means percent inhibition Concentration mol./l.

PREPARATION A Ethyl p-arnino-fl-arylacrylates Employing the procedure of Example IA, which is essentially that taught by Lukes, et al., Chem. Listy, 50, 278 (1956), (C.A. 50, 7796d), the following arylacrylates not previously reported in the literature are synthesized:

PREPARATION B 4-hydroxy-6-arylpyrimidines The following 4-hydroxy-6-arylpyrimidines, previously unreported in the chemical literature, are prepared from the requisite starting materials employing the reaction procedures of Examples I-B and III-B.

1- and 2-napthyl 2- and 3-indolyl 2- and 3-benzoiuryl 3, 4- and fi-nitro-Z-pyridyl 4-, 5- and fi-nitro-Ei-pyrldyl 2- and 3-nitro-4-pryidyl 0, m and D-CH3OC H4 0, m and IJ-CHaCaH 3,4-(CH OhCnH3 2-thienyl 2- and 3-benzothienyl 35 PREPARATION C 4-chloro-G-arylpyrimidines Following the experimental procedures of Examples IC and HG the following 4-chloro-6-arylpyrimidines, unreported in the literature, are prepared:

1- and Z-naphthyl 2- and 3-indo1yl 2- and 3-benzothlenyl 4-, 5- and 6-NOz-3-pyrldyl 2- and 3-NO2-4-pyridy1 PREPARATION D Ethyl aroylacetates (a) Ethyl l-naphthoylacetate.-To 3.62 g. of sodium dissolved in 125 ml. of absolute ethanol is added 20.4 g. of ethyl acetoacetate and the mixture cooled to C. while 15.35 g. of naphthoyl chloride in 75 ml. of benzene is added with stirring. After 30 minutes, solutions of 3.62 g. of sodium in 125 ml. of ethanol and 15.35 g. of naphthoyl chloride in 75 ml. of benzene are added simultaneously to the reaction mixture. The precipitate is filtered, taken up in several volumes of water and treated with a 10% cupric acetate solution. The precipitated copper complex (23 g.) is decomposed with 20% sulfuric acid to provide 25.5 g. of ethyl a-(l-naphthoyDacetoacetate which in turn, on treatment with ammonium hydroxide provides the desired product.

The following ethyl aroylacetates not previously reported in the literature are synthesized by the aforedescribed procedure, which is essentially that taught by Libermann, et al., Bull. soc. chim. France, 486 (1950), or by techniques outlined by Hauser, et al., Organic Reactions, John Wiley & Sons., Inc., New York, vol. I, Chapter 9, p. 266:

O O Ar-QJ CH2 -O C2115 2 and 3-benzofuryl 2- and 3-NOr4-Dyridyl PREPARATION E 2-mercapto-4-hydroxy-6-arylpyrimidines The following 6-aryl-2-thiouracil intermediates, not previously reported in the literature, are prepared by repe- 36 tition of the procedure of Example IIIA starting with the appropriate reagents:

0, m and p-HOzCCaH; o and p-CNC H,

2- and 3-furyl 2- and 3-indolyl PREPARATION F Following the procedure of Example II-A and starting with the requisite nitrochlorobenzonitrile the following 2- carbomethoxy-3-aminobenzothiophenes not previously reported in the chemical literature are prepared:

X=4NO2 and 6NO2 PREPARATION G Starting with 4- and 6-nitro-2-carbometh0xy-3-aminobenzothiophene and employing the procedure of Example II-B the following 4-hydroxybenzothien0-[3,2-d1pyrimidines, not previously reported in the literature, are

and PREPARATION H The procedure of Example II-C is repeated, starting with 7- and 9-nitro-4-hydroxy-benzothieno[3,2-d1pyrimidine, to provide the following 4-chloro-benzothieno[3,2-d]

pyrimidines, previously unreported in the chemical literature:

X=7NO and 9--N0 PREPARATION I 4-aminobenzothieno[3,2-d] pyrimidines Employing the experimental procedures of Example II-D, the following previously unreported 4-aminobenzothieno[3,2-d]pyrimidines are synthesized starting from the appropriate intermediates:

1. A compound selected from those of the formula:

and the acid addition salts thereof, wherein:

Ar is selected from the group consisting of phenyl; substituted phenyl wherein said substituent is methyl, methoxy, 3,4-dimethoxy, hydroxy, trifluoromethyl, fluorine, chlorine, bromine, carboxy, cyano, nitro, dialkylamino said alkyl containing from 1 to 3 carbon atoms; amino or alkanoylamino containing from 1 to 4 carbon atoms; pyridyl; thienyl; furyl; monosubstituted pyridyl, thienyl or furyl wherein said substituent is alkanoylamino containing from 1 to 4 carbon atoms; naphthyl; 3-indolyl; 2- and 3-benzothienyl; and 2- and 3-benzofuryl;

R and R when considered separately are each selected from the group consisting of hydrogen provided that when one of said R and R substituents is hydrogen, the other is a member selected from the group consisting of alkyl containing from 2 to 4 carbon atoms, substituted ethyl wherein said substituent is selected from the group consisting of 2-dimethylamino, 2-hydroxy and 2,2,2-trifiuoro, alkenyl containing from 3 to 4 carbon atoms, pyridylrnethyl, 2-monosubstituted phenyl wherein said substituent is carboxy or sulfamoyl and cycloalkyl containing from 3 to 7 carbon atoms; alkyl containing from 2 to 4 carbon atoms; substituted ethyl wherein said substituent is selected from the group consisting of 2- dimethylamino, 2 hydroxy and 2,2,2 trifluoro; alkenyl containing from 3 to 4 carbon atoms; pyridylmethyl; 2-monosubstituted phenyl wherein said substituent is carboxy or sulfamoyl; and cycloalkyl containing from 3 to 7 carbon atoms;

R and R when taken together with the nitrogen atom to which they are attached form a heterocyclic ring of the formula:

wherein Z is selected from the group consisting of CH 0, S and N-alkyl containing from 1 to 3 carbon atoms; and n and m are integers of from 2 to 3.

R is alkyl containing from 1 to 4 carbon atoms.

3. 4-diethylamino-6-(m-acetylaminophenyl)pyrimidine.

4. 4-diethylamino-6-(m-isobutrylaminophenyl)pyrimidine.

5. 4-diethylamino-6-(m-propionylaminophenyl)pyrimidine.

6. 4-diethylamino-6-(2-furyl)pyrimidine.

7. 4-diethylamino-6-(2-thieny1)pyrimidine.

8. 4-diethylamino-6-(p-methoxyphenyl)pyrimidine.

9. 4-diethylamino 6-phenylpyrimidine.

10. 4 diethylamino 6 (m-dimethylaminophenyl) pyrimidine.

11. 4 diethylamino 6 (p-acetylaminophenyDpyrimidine.

12. A compound of claim 1 wherein R is n-propyl and R is alkyl containing from 1 to 4 carbon atoms.

13. 4-(ethyl-n-propylamino)-6-phenylpyrimidine.

14. 4-di n propylamino 6 (m-acetylaminophenyl) pyrimidine.

15. A compound of claim 1 wherein Ar is phenyl and R is ethyl.

16. 4-[ethyl(2 hydroxyethyl)amino] 6 phenylpyrimidine.

17. 4-ethylamino-6-phenylpyrimidine.

18. A compound of claim 1 wherein Ar is phenyl and R is 2,2,2-trifiuoroethyl.

19. 4-(2,2,2 trifluoroethylamino) 6 phenylpyrimidine.

References Cited UNITED STATES PATENTS 1,915,334 6/1933 Salzberg et a1 260256.4 2,075,359 3/1937 Salzberg et a1 260256.4 2,418,548 4/ 1947 Davies et a1. 260256.4 2,425,320 8/1947 Hill 260256.4 2,606,155 8/1952 Hill 260256.4 2,735,225 2/ 1956 Goodhue et a1. 260256.4

OTHER REFERENCES Bredereck et al., Ben, 90, 942 (1957). Van Der Plas, Rec. Trav. Chim., 84, 1101 (1965).

ALEX MAZEL, Primary Examiner R. J. GALLAGHER, Assistant Examiner US. Cl. X.R.

260243 B, 247.1, 247.2 R, 247.5 R, 251 R, 251 A, 256.4 N, 330 S, 471 R; 124200, 241, 248, 251 

